GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **551 - 575** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
55301	oleoyl-ACP hydrolase	OLAH Aliases: FLJ11106 S-acyl fatty acid synthase thioesterase, medium chain SAST oleoyl-acyl-carrier-protein hydrolase	Homo sapiens (human)	migraine
8473	O-linked N-acetylglucosamine (GlcNAc) transferase	OGT Aliases: FLJ23071 HRNT1 MGC22921 O-GLCNAC OGT1 UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome Zollinger-Ellison syndrome amblyopia aortic valve disease 2 aortic valve stenosis autoimmune hepatitis breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration chromophobe renal cell carcinoma chronic ulcer of skin clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure cryptorchidism diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma dissociated nystagmus embryoma heart disease hepatitis C hepatocellular carcinoma hyperinsulinism hypospadias intellectual disability large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver carcinoma liver cirrhosis microcephaly microphthalmia myoepithelioma neurodegenerative disease non-syndromic X-linked intellectual disability 106 nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma spontaneous ocular nystagmus steatotic liver disease stomach cancer stomach carcinoma strabismic amblyopia tauopathy type 2 diabetes mellitus
4968	8-oxoguanine DNA glycosylase	OGG1 Aliases: 8-hydroxyguanine DNA glycosylase HMMH HOGG1 MUTM OGG1 type 1d OGG1 type 1e OGG1 type 1g OGG1 type 1h OGH1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Holt-Oram syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Trenaunay syndrome Langerhans-cell histiocytosis Marfan syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Rubinstein-Taybi syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia VACTERL association Werner syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute chest syndrome acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adult hepatocellular carcinoma age related macular degeneration allergic asthma anal carcinoma in situ angiomyolipoma angle-closure glaucoma anthracosilicosis anthracosis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial infectious disease bacterial meningitis basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder transitional cell papilloma bone marrow cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cataract central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism distal arthrogryposis duodenum disease dysthymic disorder embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exocrine pancreatic insufficiency familial adenomatous polyposis 1 familial adenomatous polyposis female breast carcinoma follicular adenoma follicular lymphoma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gallbladder disease gastric cardia adenocarcinoma gastric diffuse adenocarcinoma gastrointestinal system cancer gestational diabetes glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperglycemia hypertension hyperthyroidism idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor keratosis kidney angiomyolipoma kidney cancer kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leiomyoma leukemia liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus nephritis lymphoma macular degeneration major depressive disorder male infertility melancholic depression melanoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia with limb anomalies middle cerebral artery infarction mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelodysplastic syndrome myeloid sarcoma myeloproliferative neoplasm myocardial infarction myofibroma nail-patella syndrome nasopharynx carcinoma nephritis nephroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete ymphosarcoma oral mucosa leukoplakia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis pre-eclampsia primary angle-closure glaucoma primary open angle glaucoma prion disease progeria progressive supranuclear palsy propionic acidemia prostate cancer prostate carcinoma pterygium pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis senile cataract silent myocardial infarction situs inversus skin benign neoplasm skin cancer skin disease skin melanoma split hand-foot malformation 1 with sensorineural hearing loss sporadic breast cancer squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomach disease systemic lupus erythematosus thrombocytopenia-absent radius syndrome thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicocele vertebrobasilar insufficiency viral meningitis white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
55753	oxoglutarate dehydrogenase L	OGDHL Aliases: FLJ10851	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome breast cancer cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma eosinophilic esophagitis hepatocellular carcinoma large intestine cancer liver cancer oxoglutarate dehydrogenase deficiency pancreatic cancer pancreatic carcinoma
4967	oxoglutarate dehydrogenase	OGDH Aliases: E1k KGD1 OGDC-E1 OGDH2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Laron syndrome Leigh disease Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome achondroplasia alternating hemiplegia of childhood arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer cancer central nervous system disease cerebral degeneration colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease embryoma hydrocephalus lactic acidosis large intestine cancer lingual-facial-buccal dyskinesia movement disease nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus oxoglutarate dehydrogenase deficiency phenylketonuria placental insufficiency primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency senile degeneration of brain status epilepticus urea cycle disorder viral infectious disease
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus visual epilepsy
4952	OCRL inositol polyphosphate-5-phosphatase	OCRL Aliases: Dent disease 2 Dent-2 OCRL1	Homo sapiens (human)	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy
4938	2'-5'-oligoadenylate synthetase 1	OAS1	Homo sapiens (human)	primary immunodeficiency disease
221443	O-acyl-ADP-ribose deacylase 1	OARD1 Aliases: MGC19570 TARG1 dJ34B21.3 terminal ADP-ribose protein glycohydrolase 1	Homo sapiens (human)	acute myeloid leukemia neurodegenerative disease stomach cancer stomach carcinoma
60506	nyctalopin	NYX Aliases: CLRP CSNB1A	Homo sapiens (human)	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
11164	nudix hydrolase 5	NUDT5 Aliases: YSA1H hYSAH1	Homo sapiens (human)	breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
50863	neurotrimin	NTM Aliases: CEPU-1 HNT IGLON2 IgLON family member 2 NTRI neurotrimin	Homo sapiens (human)	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
4913	nth like DNA glycosylase 1	NTHL1 Aliases: NTH1 OCTS3	Homo sapiens (human)	B-cell lymphoma Fanconi anemia complementation group D2 Fanconi anemia Langerhans-cell histiocytosis acoustic neuroma actinic keratosis adenocarcinoma adenoma angiomatous meningioma autosomal recessive intellectual developmental disorder basal cell carcinoma benign meningioma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma clear cell meningioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatosis papulosa nigra duodenum adenocarcinoma embryoma endometrial cancer endometrial carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 3 familial adenomatous polyposis fibrous meningioma follicular adenoma intraorbital meningioma intraventricular meningioma inverted follicular keratosis islet cell tumor large intestine cancer laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma melanoacanthoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma non-Hodgkin lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cyst pancreatic adenocarcinoma papillary adenoma parasagittal meningioma pituitary adenoma psammomatous meningioma rectal benign neoplasm rectum cancer reticulosarcoma sarcomatoid carcinoma seborrheic dermatitis seborrheic keratosis secretory meningioma skin benign neoplasm skin cancer skin disease spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma transitional meningioma tuberous sclerosis 2 tuberous sclerosis urinary bladder cancer uterine corpus cancer
56953	5',3'-nucleotidase, mitochondrial	NT5M Aliases: dNT-2 dNT2 mdN	Homo sapiens (human)	Miller-Dieker lissencephaly syndrome Smith-Magenis syndrome
4907	5'-nucleotidase ecto	NT5E Aliases: CALJA CD73 eN eNT	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Baraitser-Winter syndrome Chagas disease Crohn's colitis Crohn's disease Down syndrome Fabry disease Fraser syndrome 1 Fraser syndrome Gilbert syndrome Goldenhar syndrome Goodpasture syndrome Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Jervell-Lange Nielsen syndrome Kallmann syndrome MHC class II deficiency Meniere's disease Moebius syndrome Muckle-Wells syndrome Muenke Syndrome Nance-Horan syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Takayasu's arteritis Troyer syndrome Turner syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome X-linked agammaglobulinemia acinar cell carcinoma acoustic neuroma acute lymphoblastic leukemia acute maxillary sinusitis acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosine deaminase deficiency adult acute lymphocytic leukemia adult epithelioid sarcoma adult lymphoma adult medulloblastoma adult respiratory distress syndrome agammaglobulinemia allergic asthma allergic rhinitis amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 angiomatous meningioma angle-closure glaucoma ankylosing spondylitis anterior horn cell disease anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arterial tortuosity syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thyroiditis autosomal recessive distal hereditary motor neuronopathy 1 basal cell carcinoma benign meningioma benign mesothelioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma brain cancer branchiootic syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma calciphylaxis cancer carcinoma cardiac arrest cardiovascular system disease cecum adenocarcinoma celiac disease central nervous system cancer central nervous system origin vertigo cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood epithelioid sarcoma childhood leukemia childhood lymphoma childhood medulloblastoma cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic lymphocytic leukemia chronic maxillary sinusitis chronic obstructive pulmonary disease chronic rhinitis chylomicron retention disease clear cell meningioma clear cell renal cell carcinoma cleft palate colitis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital hemolytic anemia congenital hypogammaglobulinemia congenital nystagmus congestive heart failure connective tissue disease corneal disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma depressive disorder diffuse large B-cell lymphoma dissociated nystagmus double outlet right ventricle dysthymic disorder embryoma encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis enthesopathy epilepsy esophagitis esophagus squamous cell carcinoma eunuchism fibromyalgia fibrous meningioma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gastritis gastroenteritis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma gonadal dysgenesis granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hepatitis hepatocellular carcinoma hereditary arterial and articular multiple calcification syndrome high grade glioma hydrocephalus hyperthyroidism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated cleft palate isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoconus keratosis follicularis kidney cancer large intestine cancer laryngeal disease laryngeal squamous cell carcinoma lateral sclerosis lipid storage disease liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma major depressive disorder malignant mesothelioma mastoiditis maxillary sinusitis medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma mongolian spot motor neuron disease mucocele of salivary gland mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis myocardial infarction neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder newborn respiratory distress syndrome non-suppurative otitis media nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea olfactory groove meningioma orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pathologic nystagmus peptic esophagitis pericarditis periodontitis peripheral nervous system disease peripheral vascular disease pituitary adenoma polyarteritis nodosa polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum psoriasis pulmonary fibrosis pustulosis of palm and sole pycnodysostosis rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma secretory meningioma senile degeneration of brain sensorineural hearing loss septooptic dysplasia severe combined immunodeficiency sickle cell anemia silent myocardial infarction skin melanoma spinal meningioma spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma suppurative periapical periodontitis thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tonsillitis tracheal disease transitional meningioma trypanosomiasis tuberculosis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer vasculitis vasomotor rhinitis visual epilepsy
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL Aliases: H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Homo sapiens (human)	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
123904	neuritin 1 like	NRN1L Aliases: MRCC2446 UNQ2446	Homo sapiens (human)	epilepsy visual epilepsy
9572	nuclear receptor subfamily 1 group D member 1	NR1D1	Homo sapiens (human)	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
4886	neuropeptide Y receptor Y1	NPY1R	Homo sapiens (human)	amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
80896	N-acetylneuraminate pyruvate lyase	NPL Aliases: DHDPS1 NPL1 dihydrodipicolinate synthetase homolog 1 (E. coli)	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Crohn's colitis Crohn's disease Ewing sarcoma Pick's disease Reye syndrome alcohol dependence alcohol use disorder atopic dermatitis bipolar disorder cerebral degeneration cholestasis congestive heart failure dermatitis epilepsy essential hypertension generalized epilepsy with febrile seizures plus hypertension idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease influenza juvenile myoclonic epilepsy myopathy obsolete major affective disorder 1 obsolete major affective disorder 2 panic disorder prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss ulcerative colitis visual epilepsy
4864	NPC intracellular cholesterol transporter 1	NPC1 Aliases: SLC65A1	Homo sapiens (human)	Niemann-Pick disease type C1 Niemann-Pick disease
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Homo sapiens (human)	Lafora disease
55768	N-glycanase 1	NGLY1 Aliases: FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	Homo sapiens (human)	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
129807	neuraminidase 4	NEU4	Homo sapiens (human)	cancer embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma

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